Computational Fontan Analysis: Preserving Accuracy While Expediting Workflow

Author:

Liu Xiaolong12,Aslan Seda12,Kim Byeol12,Warburton Linnea2,Jackson Derrick2,Muhuri Abir2,Subramanian Akshay2,Mass Paige3,Cleveland Vincent3,Loke Yue-Hin4,Hibino Narutoshi5,Olivieri Laura34,Krieger Axel12

Affiliation:

1. Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, USA

2. Department of Mechanical Engineering, University of Maryland, College Park, MD, USA

3. Sheikh Zayed Institute for Pediatric Surgical Innovation, Children’s National Medical Center, Washington, DC, USA

4. Division of Cardiology, Children’s National Medical Center, Washington, DC, USA

5. Department of Cardiac Surgery, University of Chicago/Advocate Children’s Hospital, Chicago, IL, USA

Abstract

Background: Postoperative outcomes of the Fontan operation have been linked to geometry of the cavopulmonary pathway, including graft shape after implantation. Computational fluid dynamics (CFD) simulations are used to explore different surgical options. The objective of this study is to perform a systematic in vitro validation for investigating the accuracy and efficiency of CFD simulation to predict Fontan hemodynamics. Methods: CFD simulations were performed to measure indexed power loss (iPL) and hepatic flow distribution (HFD) in 10 patient-specific Fontan models, with varying mesh and numerical solvers. The results were compared with a novel in vitro flow loop setup with 3D printed Fontan models. A high-resolution differential pressure sensor was used to measure the pressure drop for validating iPL predictions. Microparticles with particle filtering system were used to measure HFD. The computational time was measured for a representative Fontan model with different mesh sizes and numerical solvers. Results: When compared to in vitro setup, variations in CFD mesh sizes had significant effect on HFD ( P  =  .0002) but no significant impact on iPL ( P  =  .069). Numerical solvers had no significant impact in both iPL ( P  =  .50) and HFD ( P  =  .55). A transient solver with 0.5 mm mesh size requires computational time 100 times more than a steady solver with 2.5 mm mesh size to generate similar results. Conclusions: The predictive value of CFD for Fontan planning can be validated against an in vitro flow loop. The prediction accuracy can be affected by the mesh size, model shape complexity, and flow competition.

Funder

National Institutes of Health

National Heart, Lung, and Blood Institute

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,General Medicine,Pediatrics, Perinatology and Child Health,Surgery

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